Familial hypercholesterolemia
Protein losing enteropathy
Lynch Syndrome Multi Gene Panel (MLH1, MSH2, MSH6, PMS2 and EPCAM), Genomic Unity®
Mental Health (Psychotropic) Pharmacogenetics (PGx) Gene Variation Panel
Pneumocystis pneumonia
Coccidioidomycosis
Syndrome of inappropriate antidiuretic hormone secretion (SIADH)
Medium-Chain Acyl-CoA Dehydrogenase (MCAD) Mutation Analysis
Hepatitis Be Antigen
Muscle-Specific Kinase (MuSK) Autoantibody
LDS
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Lysosomal Storage Disease Gene Mutation Panel, NGS
All
Diseases
Overview
Clinical Utility
Interpretation
Reference Ranges
Methodology
Specimen Collection
Additional Testing
Turnaround Time
CPT
ICD10
Additional ICD10
References
All
Diseases
Overview
Clinical Utility
Interpretation
Reference Ranges
Methodology
Specimen Collection
Additional Testing
Turnaround Time
CPT
ICD10
Additional ICD10
References
Lysosomal Storage Disease Gene Mutation Panel, NGS
Medical Test
Methodology
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Lysosomal Storage Disease Gene Mutation Panel, NGS
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